Bulletin of the Chemical Society of Japan p. 2521 - 2529 (2000)
Update date:2022-08-03
Topics:
Koto
Hirooka
Yoshida
Takenaka
Nagamitsu
Sakurai
Zen
Yago
Tomonaga
Two-step conversions of myo-inositol into (±)-2,3,4,5,6- and 1,3,4,5,6-penta-O-benzyl-myo-inositols are described. Starting from these monohydroxy derivatives of myo-inositol, O-β-L-arabinopyranosyl-(1→2)-sn-myo-inositol from Japanese green tea, Camellia sinensis, and O-α-D-galactopyranosyl-(1→3)-sn-myo-inositol (galactinol) as well as its homolog, O-α-D-galactopyranosyl-(1→6(II))-galactinol, were synthesized by way of the in situ activating glycosylation procedure.
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Doi:10.1021/jo01274a005
(1968)Doi:10.1021/ja00483a026
(1978)Doi:10.1002/jhet.5570320525
(1995)Doi:10.1002/cber.19671000812
(1967)Doi:10.1021/ja00056a013
(1993)Doi:10.1021/om9507282
(1996)